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1213497-62-1

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1213497-62-1 Usage

General Description

"(1S)-1-(2-Methylphenyl)butylamine HCl" is a chemical compound that is also known as (S)-alpha-Methylbenzylamine hydrochloride. It belongs to the class of organic compounds known as benzene and substituted derivatives which include molecules containing one or more benzene rings. This chemical is used mainly in the research and development phase in laboratories, particularly in the synthesis of more complex chemical structures. As a hydrochloride salt, it's highly soluble in water, making it easier to handle. Like many lab chemicals, it needs to be handled with appropriate safety measures to prevent exposure and possible harm.

Check Digit Verification of cas no

The CAS Registry Mumber 1213497-62-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,3,4,9 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1213497-62:
(9*1)+(8*2)+(7*1)+(6*3)+(5*4)+(4*9)+(3*7)+(2*6)+(1*2)=141
141 % 10 = 1
So 1213497-62-1 is a valid CAS Registry Number.

1213497-62-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-1-(o-Tolyl)butan-1-amine hydrochloride

1.2 Other means of identification

Product number -
Other names (1S)-1-(2-methylphenyl)butan-1-amine,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1213497-62-1 SDS

1213497-62-1Downstream Products

1213497-62-1Relevant articles and documents

Synthesis of enantiopure 1-aryl-1-butylamines and 1-aryl-3-butenylamines by diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine amide

Dalmolen, Jan,Van Der Sluis, Marcel,Nieuwenhuijzen, Jose W.,Meetsma, Auke,De Lange, Ben,Kaptein, Bernard,Kellogg, Richard M.,Broxterman, Quirinus B.

, p. 1544 - 1557 (2007/10/03)

The synthesis of enantiopure 1-aryl-1-butylamines via a highly diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine amide is reported. These are synthesised by a three-step procedure, which involves: (a) formation of the chiral imines; (b) asymmetric addition of the allylzinc reagent; (c) removal of the chiral auxiliary by means of a reductive or non-reductive method. The reductive method provides 1-aryl-1-butylamines whereas the non-reductive method preserves the double bond to afford 1-aryl-3-butenylamines. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

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